Oncolytic viro-chemotherapy exhibits antitumor effect in laryngeal squamous cell carcinoma cells and mouse xenografts

Abstract

Background: Oncolytic virus can specifically replicate in and then lyse tumor cells, but seldom in normal cells. Further studies have shown the significant therapeutic effect of oncolytic virotherapy combining with other strategies, such as chemo-, radio-, and immunotherapy et al. In this study, we investigated the combinational effect of oncolytic virus ZD55-TRAIL and chemotherapy drug doxorubicin (DOX) on human laryngeal squamous cell carcinoma (LSCC).

Methods: The effect of ZD55-TRAIL combined with DOX on cell growth was assessed in LSCC Hep2 cells and normal cells by MTT assay. Hochest 33342 staining was performed to observe cell morphological changes. Western blot was used to detect the expression of apoptotic activation proteins. The in vivo antitumor efficacy of combination treatment was estimated in laryngeal cancer xenograft models.

Results: The combination of ZD55-TRAIL and DOX exhibited enhanced inhibitory effects on laryngocarcinoma cell growth, and had few side effects to normal cells in vitro. Chemotherapy drug increased the inducement of tumor cell apoptosis mediated by oncolytic virus. In vivo experiment confirmed that the combination treatment significantly inhibited Hep2 laryngocarcinoma xenografts growth in mice.

Conclusion: The oncolytic viro-chemotherapy is a potent therapeutic approach for in vitro cytotoxicity evaluation of Hep2 cells and xenograft growth in vivo.

Keywords:

• laryngocarcinoma
• oncolytic virus
• ZD55-TRAIL
• doxorubicin

Introduction

Human laryngeal squamous cell carcinoma (LSCC) is the sixth most common cancer worldwide with high morbidity and mortality, which is a serious threat to human health. ¹ The incidence rate is about 16%~40% of systemic malignant tumors according to the National Cancer Institute Data of Surveillance, Epidemiology, and End Results (SEER). ^2,3 In the United States, >55,000 new cases of LSCC were found each year, and among them 12,000 were dead. ^2,4 Although the development of early detection technique largely improved laryngeal cancer diagnosis and prognosis, it is still hard to eradicate the high-grade laryngeal cancer. ⁵ Therefore, novel therapeutic strategies for LSCC are urgently needed.

Recently, oncolytic virotherapy has attracted great attention since oncolytic virus can specifically proliferate in and finally lyse tumor cells. ^6–8 Even a small quantity of oncolytic virus can selectively spread to surrounding tumor cells. ^9,10 Up to date, >12 different oncolytic viruses are undergoing Phase I–III clinical trials for treatment of various types of cancers,¹¹ including adenovirus, poxvirus, herpes simplex virus (HSV), and reovirus. ^12,13 In particular, the first authorized oncolytic virus agent by US Food and Drug Administration, Talimogene laherparepvec (T-VEC), which is a genetically modified HSV delivering granulocyte macrophage colony-stimulating factor (GM-CSF), improved durable response rate in patients with advanced melanoma in a Phase III trial. ¹⁴ Further studies have shown the significant therapeutic effect of oncolytic virotherapy combining with other strategies such as chemo-, radio-, and immunotherapy. ¹⁵

In our previous studies, although oncolytic adenovirus acquired a great achievement focusing on treating solid tumors,^16,17 the antitumor effect of adenovirus particles alone is limited. It makes us explore more effective regime, such as oncolytic viro-chemotherapy and viro-radiotherapy. To be noted, the combined therapy indeed made great progress in preclinical or clinic cancer trials. ¹⁸ The oncolytic adenoviruses include ZD55-TRAIL, H101, AD5/3.2xTyr,¹⁹ CRAdRGDflt-IL24,²⁰ Ad5/5-D24^21, and SG600. ²² ZD55-TRAIL, an E1B55K gene-deleted oncolytic adenovirus harboring tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) constructed by us, exerted efficient cancer therapy effect. ²³

TRAIL is a member of the tumor necrosis factor family that selectively induces apoptosis in tumor cells but not in most normal cells. However, tumor cells represent resistance to TRAIL. As a traditional chemotherapy drug, doxorubicin (DOX) could inhibit tumor cell cycle and induce apoptosis in a wide-broad human tumors,^24,25 but chemotherapy could cause side effect to normal cells. Therefore, how to improve cell sensitivity to TRAIL and reduce DOX toxic effect is needed to solve. In this study, we investigated the therapeutic effect of ZD55-TRAIL combining with DOX in LSCC. The results showed that the combination treatment effectively inhibited tumor growth both in vitro and in vivo, enhanced tumor cell apoptosis, and decreased the toxicity effect on normal cells in vitro by reducing DOX dosage.

Materials and methods

Cell lines and viruses

HEK293 cell line was obtained from Microbix Biosystems Inc. (Toronto, Ontario, Canada). Human normal liver cell line L-02 and human LSCC cell line Hep2 were purchased from the Shanghai Cell Collection (Shanghai, China). HEK293 and L-02 cells were cultured in DMEM (GIBCO BRL, Grand Island, NY, USA) supplemented with 10% heat-inactivated FBS (GIBCO BRL). Hep2 cells were cultured in 1640 supplemented with 10% FBS. All cells were cultured in a 5% CO₂ humidified incubator at 37°C.

ZD55-TRAIL, ZD55-enhanced green fluorescent protein (EGFP) virus was amplified in HEK293 cells, and the large-scale purification was performed by ultracentrifugation in a cesium chloride gradient, followed by dialysis. Virus titer was determined by TCID50 assay in HEK293 cells. EGFP expression was observed by fluorescence microscope (IX71-22FL/PH, Olympus Corporation, Tokyo, Japan), and the percentage of EGFP-positive cells was measured by flow cytometry.

Comparative replication assay

To determine the relative replication efficiency of virus, Hep2 cells were infected with ZD55-TRAIL, ZD55-TRAIL plus DOX in a humidified chamber at 37°C with 5% CO₂ air and maintained for 48 hrs. The progeny virus was collected from supernatant for virus titer determination.

Assessment of viral E4 levels

Total DNA was obtained from each sample using FastPure cell/tissue DNA isolation mini kit (Vazyme, Nanjing, China). E4 gene was measured by quantitative real-time PCR and normalized with a standard. Standard curves were generated by serial dilutions of pAdeasy-1, which is a 33.4 kb plasmid containing most of the human adenovirus serotype V genome (ThermoFisher scientific, Waltham, MA, USA). The primers sequences are: E4, forward 5ʹ-CTAACCAGCGTAGCCCCGA-3ʹ and reverse 5ʹ-TGAGCAGCACCTTGCATTTT-3ʹ; GAPDH, forward 5ʹ-ATTCCACGGCACAGTCAAGG-3ʹ and reverse 5ʹ-ACATACTCAGCACCAGCATCG-3ʹ. All the reactions were done in triplicates.

Assessment of TRAIL mRNA expression

Total RNA was extracted from each sample to assess for TRAIL levels using quantitative real-time PCR. TRIzol reagent (ThermoFisher) was used for RNA isolation. Single-strand cDNA was synthesized using ReverTra Ace qPCR RT Kit (Toyobo, Osaka, Japan), and SuperReal Premix plus (Vazyme) was used for amplification. The primer sequences are: TRAIL, forward 5ʹ-TGCGTGCTGATCGTGATCTTC-3ʹ and reverse 5ʹ-GCTCGTTGGTAAAGTACACGTA-3ʹ. All the reactions were done in triplicates, and the results obtained for TRAIL were normalized to GAPDH.

Cell viability assay

Cells were seeded in 96-well plates for 12 hrs, and then treated with ZD55-TRAIL, DOX, ZD55-TRAIL plus DOX. At the indicated time points after treatment, the medium was removed and fresh medium containing (MTT, 0.5 mg/mL) was added to each well. After 4 hrs in the incubator, the supernatant was removed and 150 μL dimethyl sulfoxide was added to each well. Absorbance was read at 490 nm with a microplate reader (TECAN, Grödig, Austria).

Western blot analysis

Total proteins were collected by cell lysis buffer (Beyotime, Nantong, China). Protein concentrations were determined by Pierce BCA protein assay kit (ThermoFisher scientific). Proteins were separated by SDS-PAGE on an 8–12% gel and then transferred to a 0.45 μm nitrocellulose membrane (Millipore Corp., Bedford, MA, USA). After being blocked in blocking buffer (5% bovine serum albumin, 10 mmol/L Tris–HCl, pH 8.0, 150 mmol/L NaCl, and 0.05% Tween20), the membranes were incubated with primary antibodies and the corresponding secondary fluorescent antibodies (LI-COR Biosciences Inc., Lincoln, NE, USA). The fluorescent signal was detected by the Odyssey infrared imaging system (LI-COR Biosciences Inc.). The primary antibody anti-E1A, TRAIL, Bax, and GAPDH were purchased from Santa Cruz Biotechnology (Santa Cruz, CA, USA). XIAP, PARP, and caspase-8 antibodies were purchased from Cell Signaling Technology (Danvers, MA, USA).

Cytopathic assay

Hep2 cells were grown in 48-well plates, then treated with ZD55-TRAIL, DOX, ZD55-TRAIL plus DOX. Two days later, cells were exposed to 2% crystal violet in 20% methanol for 15 mins and then washed with distilled water and documented by photography. Uninfected cells served as control.

Hochest33342 staining

Cells were seeded in 6-well plates at a density of 2.5×10⁵ per well overnight. 48 hrs after treatment, cells were incubated with 1 µg/µL hochest33342 (Beyotime) for 15 mins, washed twice with ddH₂O, and observed under a fluorescence microscope.

Flow cytometric analysis

Adherent cells were trypsinized and harvested at 48 hrs after treatment. Apoptosis cells were detected using Annexin-V-fluorescein isothiocyanate (FITC) and propidium iodide (PI) double staining following the manufacturer's (Beyotime).

Animal experiments

4– to 5-week-old female BALB/c nude mice were purchased from the Shanghai Animal Experimental Center of the Chinese Academy of Sciences. The present study was approved by the ethics committee of College of Life Sciences, Zhejiang Sci-Tech University. All procedures in animal experiments were performed according to institutional guidelines and conformed to the National Institutes of Health guidelines on the ethical use of animals. 5×10⁶ Hep2 cells were subcutaneously injected into the right flank of nude mice. When tumor volumes reached 70–100 mm³, the mice were randomly divided into four groups. The mice borne with tumors were treated with ZD55-TRAIL, DOX, ZD55-TRAIL combined with DOX or PBS, respectively. Total 1×10⁹ plaque-forming units (PFUs) ZD55-TRAIL were injected into each mouse via an intratumoral manner for three times every other day, while DOX was injected into the peritoneal cavity at a dose of 4 mg/kg body weight for three consecutive days. Tumor size was measured by a vernier caliper every 3 or 4 days. Tumor volume (V) was calculated according to the formula: V (mm³)=1/2× length × width × width.

H&E staining and TUNEL assay

Tissues were fixed in 10% formalin, dehydrated with graded concentrations of ethanol, and embedded in paraffin wax. The sections were stained with HE for histological analysis. For TUNEL assay, an in situ apoptosis detection kit (Sino-American Biotechnology Co., Luoyang, China) was used.

Briefly, tumor sections were incubated with proteinase K (Merck Co., Darmstadt, Germany) and rinsed with ddH₂O, then dewaxed with dimethylbenzene, and rehydrated with gradient ethanol twice, each for 5 mins. Endogenous peroxidase was blocked with 3% H₂O₂, and sections were incubated with equilibration buffer and terminal deoxynucleotidyl transferase (TdT) enzyme. Finally, the sections were incubated with antidigoxigenin–peroxidase conjugate. Peroxidase activity in each tissue section was shown by the application of DAB (peroxidase substrate kit, Sino-American Biotechnology). Hematoxylin was used as a counterstain.

Statistical analysis

The combined effects of DOX and ZD55-TRAIL on cell viability were analyzed with the median-effect methods of Chou and Talalay²⁶ using CalcuSyn software (Biosoft, Ferguson, MO, USA). The combination index (CI) values were used to evaluate the interaction between the drug and virus. For the fraction of virus affected combination index (Fa-CI) plot analysis, CI <1, =1, and >1 is defined as synergism, additive effect, and antagonism, respectively. The data were confirmed with the isobologram method. ^27,28

The experimental statistical significance was analyzed by Graph Pad 6.0 software and Student’s t-test. When p<0.05, it is considered statistically significant.

Results

Characterization of ZD55-TRAIL in laryngocarcinoma cells

Oncolytic viral vector ZD55 was constructed based on adenovirus serotype V with an E1B 55-kDa gene deletion, enabling selective replication in many types of tumor cells. ¹⁵ ZD55-TRAIL was obtained by inserting TRAIL gene expression frame into the deleted E1B 55-kDa region under the control of human cytomegalovirus immediate-early (CMV-IE) promoter (Figure 1A). Hep2 cells were treated with ZD55-TRAIL, DOX, or the combination for 48 hrs. The combined treatment caused more adenovirus E1A and TRAIL protein expression in Hep2 cells than those in ZD55-TRAIL-infected cells. There was no E1A expression in mock cells and cells treated with DOX (Figure 1B). The ZD55-TRAIL replication capacity was enhanced by DOX (Figure 1C). The DNA level of E4 gene, another early adenoviral gene, was higher in the combination-treatment group than ZD55-TRAIL infected group (Figure 1D).

Figure 1 Characterization of oncolytic adenovirus ZD55-TRAIL. (A) The diagram of adenovirus. WT, wild type. ITR, inverted terminal repeats. (B) Identification of recombinant adenovirus by western blot analysis. ZD55-TRAIL (8MOI), DOX (0.2 μmol/L), or ZD55-TRAIL (8MOI) plus DOX (0.2 μmol/L) were used to treat Hep2 cells for 48 hrs. Collected cell proteins for analyzing the expression of E1A and TRAIL. Untreated cells served as control. GAPDH was used as a protein loading control. (C) Hep2 cells were treated as (B). The progeny virus was collected for virus titer determination. (D) E4 gene copies were determined as a measurement of viral replication. Data are presented in (C, D) as mean ± SD of three independent experiments. *p<0.05, **p<0.01.

Abbreviations: DOX, doxorubicin; TRAIL, tumor necrosis factor-related apoptosis-inducing ligand.

ZD55-TRAIL exerts synergistic effect with DOX in laryngocarcinoma cells

Hep2 cells were treated with DOX (from 0.05 μmol/L to 0.8 μmol/L), ZD55-TRAIL (from 2 MOI to 32 MOI), or a combination at the constant ratio of 1:40 for 48 hrs. The combination of ZD55-TRAIL and DOX displayed an enhanced tumor-killing effect in Hep2 cells (Figure 2A). The survival rate of cells with 0.2, 0.7, and 0.8 μmol/L DOX treatment was 76.57%, 63.01%, 59.57%, and 50.54%, 30.95%, 28.99% after 8, 28, 32 MOI of ZD55-TRAIL infection, respectively. All were higher than the survival rate of cells with the combination treatment (34.43%, 23.34%, and 20.54%) (Figure 2A). Besides, ZD55-TRAIL plus DOX indicated a synergistic antitumor effect analyzed by the median-effect methods of Chou and Talalay. We evaluated these quantitated data by Fa-Cl (Figure 2B). The X marks represented the CI values of the combination treatment groups. The CI values were 0.416, 0.381, 0.444, 0.609, and 0.55, respectively (Figure 2B). The middle curve line represented the simulated CI values of the combination treatment groups surrounded by two lines of algebraic estimations of the 95% confidence intervals. All experimental CI values at the tested ratio were significantly <1 and between the two confidence lines, indicating synergism of combination treatments. Moreover, the result of crystal violet staining for cell viability determination showed that conjugation of DOX with ZD55-TRAIL obviously inhibited cell growth (Figure 2C).

Figure 2 The combination of ZD55-TRAIL and DOX suppressed tumor cell proliferation. (A) Hep2 cells were treated with ZD55-TRAIL, DOX, or ZD55-TRAIL plus DOX for 48 hrs with the indicated dosage. Cell viability was evaluated by the MTT assay. (B) Synergistic effect of ZD55-TRAIL combined with DOX was quantified by combination index (CI) analysis and expressed as log (CI) versus fraction affected. 95% confidence intervals are shown. (C) Hep2 cells were subjected to crystal violet staining for cell viability determination 48 hrs after treatment. (D) Representative fluorescence microscope images of EGFP expression in Hep2 and L-02 cells after 10MOI ZD55-EGFP infection. (E) The percentage of EGFP-positive cells was measured by flow cytometry. (F) L-02 cells were treated with ZD55-TRAIL, DOX, or ZD55-TRAIL plus DOX for 48 hrs with the indicated dosage. Cell viability was determined by the MTT assay. (G) Expression of TRAIL mRNA was detected in Hep2 and L-02 cells using qRT-PCR at the indicated time points after 10MOI ZD55-TRAIL infection. Data are presented in (A, E, F, G) as mean ± SD of three independent experiments. **p<0.01, NS, nonsignificant.

Combination of ZD55-TRAIL and DOX does not increase cytotoxicity to normal cells

The EGFP protein expression was examined in Hep2 and liver normal L-02 cells after ZD55-EGFP virus infection, which is an oncolytic virus carrying EGFP gene. Fluorescence microscope images showed the EGFP expression in both cells and stronger expression in Hep2 cell at 48 hr time point (Figure 2D), consistent with the flow cytometry analysis results (Figure 2E). After confirmation of virus infection, it is necessary to evaluate the toxicity of ZD55-TRAIL and chemotherapeutic agent on normal cells. L-02 cells were treated with ZD55-TRAIL at different MOI, and the cell viability was detected by MTT assay. It is noticeable that the survival rate of L-02 cells kept at 84.42% after co-treated with the highest dosage of ZD55-TRAIL (30MOI) and DOX (1 μmol/l), indicating the combination treatment caused little toxic effect in L-02 cells (Figure 2F). The mRNA level of TRAIL gene was significantly higher in Hep2 cells than L-02 cells 48 hrs after infection (Figure 2G), suggesting that oncolytic virus could infect but fail to replicate in L-02 cells.

Combination of ZD55-TRAIL and DOX induces cell apoptosis

We wondered whether the antitumor effect in Hep2 cells was caused by increased cell apoptosis. First, we performed Hoechst 33342 staining to detect the morphological alterations of Hep2 cells after treatment. The results showed that co-treatment led to significant apoptosis with a feature of chromatin condensation, nuclear fragmentation, and apoptotic bodies, compared with ZD55-TRAIL or DOX-alone treated cells (Figure 3A). Annexin-V and PI staining were performed to quantify cell apoptosis. ZD55-TRAIL plus DOX caused higher ratio of apoptosis cells (33%) than ZD55-TRAIL (15.9%) and DOX (10.2%) (Figure 3B). Western blot analysis demonstrated that ZD55-TRAIL activated caspase-dependent apoptotic pathway including activation of caspase-9, and the activation could be further enhanced by DOX. Simultaneously, we found that co-treatment downregulated the expression of antiapoptosis protein XIAP and upregulated the expression of proapoptotic protein Bax (Figure 3C).

Figure 3 DOX enhanced ZD55-TRAIL-induced apoptosis in Hep2 cells. (A) Hep2 cells were infected with ZD55-TRAIL (8MOI), DOX (0.2 μmol/L), or ZD55-TRAIL (8MOI) plus DOX (0.2 μmol/l). 48 hrs later, Hep2 cells were stained with Hoechst 33342. The white arrows indicated apoptotic cells. Original magnification, 200×. (B) 48 hrs after treatment, the apoptosis of Hep2 cells was measured by flow cytometry. **p<0.01. (C) Activation of caspase-mediated apoptosis signaling pathway. Cells were treated as mentioned in (A) for 48 hrs. The expression of the indicated proteins was detected by western blot. GAPDH was used as a loading control.

Combination of ZD55-TRAIL and DOX suppresses tumor growth in vivo

The above in vitro data verified that the combination of ZD55-TRAIL and DOX had synergistic tumor cell-killing effect and induced tumor cell apoptosis. Next, we investigated the therapeutic effects of DOX and ZD55-TRAIL in nude mice. As shown in Figure 4A, the average tumor volume reached about 550 mm³ within 21 days in the control mice receiving PBS treatment, while DOX or ZD55-TRAIL suppressed tumor growth, with average tumor volume <300 mm³. ZD55-TRAIL plus DOX treatment exhibited a remarkable tumor growth suppression effect, with average tumor volume <100 mm³. It is worth mentioning that the xenograft tumors in three of eight mice in the co-treatment group were almost eradicated. We further detected cytopathic effect in vivo. The H&E staining for the liver sections showed no distinct toxicity in the combinational treatment (Figure 4B). TUNEL analysis indicated that the combination of TRAIL and DOX resulted in more cell apoptosis in tumors than that of ZD55-TRAIL or DOX alone (Figure 4B).

Figure 4 Antitumor effect of DOX and ZD55-TRAIL in Hep2 xenografts. Mice were treated with an intratumoral injection of PBS, DOX, ZD55-TRAIL, or ZD55-TRAIL followed by DOX. (A) Tumor volume was measured. *p<0.05. (B) Subcutaneous Hep2 tumors and liver tissues were performed for HE staining analysis (the upper two rows, original magnifcation: 100×). The lower row showed the cell apoptosis in tumor tissues by TUNEL assay (original magnification: 200×).

Discussion

Oncolytic virotherapy has shown promising therapeutic effects. ²⁹ The prominent advantage of this approach is that, with adding a small amount of viruses, oncolytic effects can selectively initiate anticancer action and spread to the surrounding regions. We constructed oncolytic viral vector ZD55, which is similar to ONYX-015 with an E1B 55-kDa gene deletion. The difference between them is that ZD55 has a multiple clone site and can deliver genes. ³⁰ In our previous studies, ZD55 delivered genes including TRAIL, IL-24, Smac, and XAF1. and exhibited efficient tumor-inhibition capability. ^31,32

TRAIL selectively induces apoptosis in various tumor cells and causes few toxicity to normal cells. ³³ TRAIL recognizes, binds with death receptors (DR4, DR5),³⁴ and then initiates the apoptosis signal transduction pathway. ³⁵ It has been reported that oncolytic virus ZD55-TRAIL selectively replicated in tumor cells, and the exogenous TRAIL gene did not attenuate the replication ability of the oncolytic virus. ¹⁸ However, there are several disadvantages in cancer therapy with ZD55-TRAIL, such as tumor resistance, host immune response, neutralized antibody, and unable to eliminate high-malignant tumors. ³⁶

Chemotherapeutic drugs, such as DOX, are used as an auxiliary therapeutic method for surgery in treating malignancies. ³⁷ However, the severe side effects of high-dose DOX are essential obstacles. The combination strategies with oncolytic virus and chemotherapy drugs are developed for cancer therapy. In order to obtain an enhanced or synergic therapeutic effect, it is essential to select chemotherapeutic drugs and oncolytic viruses with complementary mechanisms. Studies indicated that chemotherapy drugs upregulated death receptors (DR4 or DR5) or activated intracellular signaling pathways of TRAIL, suggesting that chemotherapy drugs may sensitize tumor cells to TRAIL-mediated apoptosis. ^35,38

Virus replication and diffusion are restricted in animal studies and clinical trials, especially when the objectives carry tumors with large masses. ^39–41 It is difficult for viruses to penetrate massive tumors, and it may be the reason for disappointing therapeutic outcomes. Therefore, exploring novel tumor biomarkers or therapeutic targets is crucial for oncolytic virus-mediated laryngeal therapy. ^42–44

In the present study, we confirmed the enhanced inhibitory effect of ZD55-TRAIL and DOX in Hep2 cells in vitro and in vivo. The results indicated that ZD55-TRAIL not only replicated, but also expressed TRAIL gene efficiently in Hep2 cells (Figures 1B and 2G). Notably, the addition of DOX was able to enhance the virus replication and TRAIL expression, and resulted in synergic inhibitory effects on the proliferation of Hep2 cells (Figures 1B–D and 2A–C). Besides, ZD55-TRAIL combined with DOX did not increase toxicity in normal liver cells in vitro (Figure 2F). Further, combination treatment induced distinct apoptosis in Hep2 cells compared with individual treatment (Figure 3).

Conclusion

The oncolytic viro-chemotherapy combining ZD55-TRAIL and DOX exerted antitumor effect in cells and in tumor xenografts in mice, indicating that the combined treatment could represent a rational approach for laryngeal cancer therapy.

Ethical approval

All applicable international, national, and/or institutional guidelines for the care and use of animals were followed.

Disclosure

The authors report no conflicts of interest in this work.

Acknowledgments

This work was supported by National Natural Science Fund (31671348, 31301064, 81573000), Zhejiang Provincial Natural Science Foundation of China (No. LY16H160056), Technology bureau of Hangzhou (No. 20130733Q36), the Grant for 521 talent project of ZSTU and Academician workstation of Zhejiang Province.